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Donnybrook Clinical Trial Associate Jobs + 30 km
No match yet? There are 30 more jobs that could match your search
As aClinical Research Associate at ICON you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. 2 years + of monitoring experience in phase I-III trials as a CRA (for a CRA II position).
As aClinical Research Associate at ICON you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. 2 years + of monitoring experience in phase I-III trials as a CRA (for a CRA II position).
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Investment Management Regulatory Specialist - Hybrid
Investment Management Regulatory Specialist - Hybrid
Deloitte Ireland LLP
County Dublin
€ Not Disclosed
Deloitte is the biggest professional services Firm in the world making an impact is more than just what we do: it's why we're here. We're driven to create positive progress for our clients, community, people, and the planet. This sense of purpose inspires us to work to the highest standards, to tackle the challenges that matter. Audit & Assurance is one of our biggest service lines and the driving engine of Deloitte Ireland. We provide services that go beyond expectations to deliver insight and confidence for our leading international and local clients. Our Audit and Assurance teams are a key part of the financial reporting ecosystem. Deloitte is constantly evolving its audit and assurance processes providing value and insights. We leverage cutting-edge technology in combination with our global network of professionals applying diverse skills and experiences to make a
Deloitte is the biggest professional services Firm in the world making an impact is more than just what we do: it's why we're here. We're driven to create positive progress for our clients, community, people, and the planet. This sense of purpose inspires us to work to the highest standards, to tackle the challenges that matter. Audit & Assurance is one of our biggest service lines and the driving engine of Deloitte Ireland. We provide services that go beyond expectations to deliver insight and confidence for our leading international and local clients. Our Audit and Assurance teams are a key part of the financial reporting ecosystem. Deloitte is constantly evolving its audit and assurance processes providing value and insights. We leverage cutting-edge technology in combination with our global network of professionals applying diverse skills and experiences to make a
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Clinical Scientist – Molecular Genetics
Clinical Scientist – Molecular Genetics
Children's Health Ireland
Dublin, County Dublin
€42,785 - €73,155 per annum
The purpose of this post is to play an integral role in the provision of the diagnostic molecular genetic service provided by the Department of Clinical Genetics. The Clinical Scientist is responsible for the selection, analysis, interpretation and accurate reporting of genetic tests as required to answer the clinical question. Excellent knowledge of clinical molecular genetics Clinical Scientist Medical Scientist Laboratory
The purpose of this post is to play an integral role in the provision of the diagnostic molecular genetic service provided by the Department of Clinical Genetics. The Clinical Scientist is responsible for the selection, analysis, interpretation and accurate reporting of genetic tests as required to answer the clinical question. Excellent knowledge of clinical molecular genetics Clinical Scientist Medical Scientist Laboratory
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Biomedical Scientist - Temporary Fixed Term 12 Months - National Donor Screening Laboratory (NDSL) National Blood Centre - The IBTS is currently recruiting a Biomedical Scientist based in the National Donor Screening Laboratory (NDSL), IBTS (incorporating the Nucleic Acid Testing (NAT), Virology and Automated Donor Grouping (ADG) laboratories). The IBTS prides itself in being a great place to work, actively promoting scientific developments and offering a good work-life balance. We are looking for a team member who enjoys the challenge of a varied working environment. * Candidates must have a relevant recognised primary degree in the field of Biomedical Science. * Excellent communication and interpersonal skills, demonstrating an ability to work in a team environment. * Excellent problem-solving skills and the ability to deduce and make rational decisions.
Biomedical Scientist - Temporary Fixed Term 12 Months - National Donor Screening Laboratory (NDSL) National Blood Centre - The IBTS is currently recruiting a Biomedical Scientist based in the National Donor Screening Laboratory (NDSL), IBTS (incorporating the Nucleic Acid Testing (NAT), Virology and Automated Donor Grouping (ADG) laboratories). The IBTS prides itself in being a great place to work, actively promoting scientific developments and offering a good work-life balance. We are looking for a team member who enjoys the challenge of a varied working environment. * Candidates must have a relevant recognised primary degree in the field of Biomedical Science. * Excellent communication and interpersonal skills, demonstrating an ability to work in a team environment. * Excellent problem-solving skills and the ability to deduce and make rational decisions.
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(Senior) Clinical Trial Manager - CNS/Rare Diseases
(Senior) Clinical Trial Manager - CNS/Rare Diseases
ICON Clinical Research Limited
County Dublin
€ Not Disclosed
Job Title: Clinical Trial Manager - CNS and Rare Diseases * Knowledge of clinical trial processes and regulations. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. * Lead clinical aspects of designated projects, ensuring adherence to budget and timelines. * Primary point of contact for the clinical aspects of designated projects and responsible for developing successful cross-functional relationships with internal and external stakeholder * Oversee clinical metrics and ensure quality standards are met. * Manage clinical project team to optimize performance and productivity. * Participate in clinical risk planning and resolut
Job Title: Clinical Trial Manager - CNS and Rare Diseases * Knowledge of clinical trial processes and regulations. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. * Lead clinical aspects of designated projects, ensuring adherence to budget and timelines. * Primary point of contact for the clinical aspects of designated projects and responsible for developing successful cross-functional relationships with internal and external stakeholder * Oversee clinical metrics and ensure quality standards are met. * Manage clinical project team to optimize performance and productivity. * Participate in clinical risk planning and resolut
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Overview - Who we are - PM Group is an employee owned, international project delivery firm with a team of 3,700 + people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. We are looking for a Lab Test Technician to join our Medical Device Client's (GMP accredited manufacturer) Research and Development team and support new product development testing & Design Verification Testing (product-injecting medical device) and day to day lab operations. Responsibilities - Daily Responsibilities * Product testing to support program milestones. * Training in appropriate test procedures and protocols as well as completion of on site complianc
Overview - Who we are - PM Group is an employee owned, international project delivery firm with a team of 3,700 + people. We are world leaders in the pharma, food, medtech and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organisations. We are focused on growing a sustainable business centred around our people, our clients and trade partners. We are looking for a Lab Test Technician to join our Medical Device Client's (GMP accredited manufacturer) Research and Development team and support new product development testing & Design Verification Testing (product-injecting medical device) and day to day lab operations. Responsibilities - Daily Responsibilities * Product testing to support program milestones. * Training in appropriate test procedures and protocols as well as completion of on site complianc
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Senior Medical Scientist - Microbiology
Senior Medical Scientist - Microbiology
St. Vincent's University Hospital SVHG St Vincent’s Holdings CLG
South Dublin, County Dublin
€ Not Disclosed
Applications are invited for the permanent position of Senior Medical Scientist - Microbiology in the Microbiology Department of St. Vincents University Hospital. Work as part of the management team in co-operation with the Consultant Head of Department, Chief Medical Scientist and Laboratory Manager to ensure the performance of the Microbiology Laboratory is professional, efficient and operates as cost effectively as possible. Work as part of a team to ensure that the Microbiology Department operates to the highest standards and that best practice is maintained and is in compliance with ISO. Identify and promote ways of raising the quality of service to patients. Informal enquiries or Role Specific Enquiries to: Ms. Abigail Salmon, Chief Medical Scientist, Microbiology as per contact details outlined on the job specification.
Applications are invited for the permanent position of Senior Medical Scientist - Microbiology in the Microbiology Department of St. Vincents University Hospital. Work as part of the management team in co-operation with the Consultant Head of Department, Chief Medical Scientist and Laboratory Manager to ensure the performance of the Microbiology Laboratory is professional, efficient and operates as cost effectively as possible. Work as part of a team to ensure that the Microbiology Department operates to the highest standards and that best practice is maintained and is in compliance with ISO. Identify and promote ways of raising the quality of service to patients. Informal enquiries or Role Specific Enquiries to: Ms. Abigail Salmon, Chief Medical Scientist, Microbiology as per contact details outlined on the job specification.
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Medical Laboratory Assistant (Aide) - MRSA
Medical Laboratory Assistant (Aide) - MRSA
St James’s Hospital
Dublin, County Dublin
€38,822 - €45,632 per annum
About us: St Jamess Hospital is Irelands largest acute academic teaching hospital and is based in Dublins south inner city. Our fundamental purpose is the delivery of health treatment, care and diagnosis as well as health promotion and preventative services at local, regional and national levels. Our academic partner is Trinity College Dublin. Medical Laboratory Aides are a key part of the laboratory team and play a significant role within the team structure in ensuring a quality and safe laboratory service is delivered. Please review the associatedRole Profilefor a detailed description of the role, as well as a full list of all eligibility criteria,qualifications and / or experience required. Also, please viewour Online Application information guide, to help guide you through the application form if needed.
About us: St Jamess Hospital is Irelands largest acute academic teaching hospital and is based in Dublins south inner city. Our fundamental purpose is the delivery of health treatment, care and diagnosis as well as health promotion and preventative services at local, regional and national levels. Our academic partner is Trinity College Dublin. Medical Laboratory Aides are a key part of the laboratory team and play a significant role within the team structure in ensuring a quality and safe laboratory service is delivered. Please review the associatedRole Profilefor a detailed description of the role, as well as a full list of all eligibility criteria,qualifications and / or experience required. Also, please viewour Online Application information guide, to help guide you through the application form if needed.
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Sr. QA Automation Engineer, Charles River Development, Assistant Vice President
Sr. QA Automation Engineer, Charles River Development, Assistant Vice President
State Street International (Ireland) Ltd
County Dublin
€ Not Disclosed
Charles River Development (CRD), a State Street Company, helps enable sound and efficient investing across all asset classes. Investment firms in more than 40 countries use Charles River IMS to manage more than US$35 Trillion in assets in the institutional investment, wealth management and hedge fund industries. Our Software as a Service-based solution (SaaS) is designed to automate and simplify investment management on a single platform - from portfolio management and risk analytics through trading and post-trade settlement, with integrated compliance and managed data throughout. Headquartered in Burlington, Massachusetts, we support clients globally with more than 750 employees in 11 regional offices. * Create comprehensive test plans with well-defined, reusable test cases from business requirements and functional specification documents.
Charles River Development (CRD), a State Street Company, helps enable sound and efficient investing across all asset classes. Investment firms in more than 40 countries use Charles River IMS to manage more than US$35 Trillion in assets in the institutional investment, wealth management and hedge fund industries. Our Software as a Service-based solution (SaaS) is designed to automate and simplify investment management on a single platform - from portfolio management and risk analytics through trading and post-trade settlement, with integrated compliance and managed data throughout. Headquartered in Burlington, Massachusetts, we support clients globally with more than 750 employees in 11 regional offices. * Create comprehensive test plans with well-defined, reusable test cases from business requirements and functional specification documents.
Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages - ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. * Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages - ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. * Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports
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They are also one of the market leaders in testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing.
They are also one of the market leaders in testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing.
11 month contract with view to extension - shift role - 4 days on 7am to 7pm and 4 days off - Purpose - The QC Microbiology Analyst role is a critically important activity to ensure efficient and effective compliant, qualification, and operation of the new strategic Drug Substance facility. This tremendous opportunity will be responsible for qualifying the Microbiology Quality Control lab and the verification of Microbiological analytical methods including but not limited to cutting edge Rapid Microbiological Methods. This person will be key in the layout of the lab testing flow to ensure the process is streamlined and in line with lean principles. Responsibilities * Perform and carry out a variety of routine microbiological analytical techniques including but not limited to environmental monitoring, WFI sampling & testing, growth promotion testing, TOC & Conductivity
11 month contract with view to extension - shift role - 4 days on 7am to 7pm and 4 days off - Purpose - The QC Microbiology Analyst role is a critically important activity to ensure efficient and effective compliant, qualification, and operation of the new strategic Drug Substance facility. This tremendous opportunity will be responsible for qualifying the Microbiology Quality Control lab and the verification of Microbiological analytical methods including but not limited to cutting edge Rapid Microbiological Methods. This person will be key in the layout of the lab testing flow to ensure the process is streamlined and in line with lean principles. Responsibilities * Perform and carry out a variety of routine microbiological analytical techniques including but not limited to environmental monitoring, WFI sampling & testing, growth promotion testing, TOC & Conductivity
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Were currently recruiting for an exciting opportunity with a Biopharmaceutical organization based in Swords. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties * Perform and carry out a variety of routine microbiological analytical techniques including but not limited to environmental monitoring, WFI sampling & testing, growth promotion testing, TOC & Conductivity testing, in-process product testing, final product testing such as bioburden and both Kinetic turbidimetric and MCS rapid endotoxin testing in compliance with GMP requirements * Perform supportive activities for general lab readiness, laboratory equipment qualification and method qualifications * To integrate and complete all documentation on time and be familiar with LIMS
Were currently recruiting for an exciting opportunity with a Biopharmaceutical organization based in Swords. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties * Perform and carry out a variety of routine microbiological analytical techniques including but not limited to environmental monitoring, WFI sampling & testing, growth promotion testing, TOC & Conductivity testing, in-process product testing, final product testing such as bioburden and both Kinetic turbidimetric and MCS rapid endotoxin testing in compliance with GMP requirements * Perform supportive activities for general lab readiness, laboratory equipment qualification and method qualifications * To integrate and complete all documentation on time and be familiar with LIMS
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Clinical Support Specialist (North Dublin, Cavan, Meath))
Clinical Support Specialist (North Dublin, Cavan, Meath))
Adecco UK Limited
County Meath
€40,000 - €50,000 per annum
They are currently seeking a Clinical Support Specialist to join the team on a permanent basis. -Support clinical training and educational workshops in key centers within the region. nurse nursing clinical
They are currently seeking a Clinical Support Specialist to join the team on a permanent basis. -Support clinical training and educational workshops in key centers within the region. nurse nursing clinical
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Sales and Clinical Support Specialist - Pain Management - Entry level
Sales and Clinical Support Specialist - Pain Management - Entry level
Recruitment Plus
Dublin, County Dublin
€ Not Disclosed
Job Title: Sales and Clinical Support Specialist - Pain Management - Entry level - Reporting to the Sales Manager, you will be responsible for clinical support and selling as part of a team within the Pain Management portfolio. You will work closely with the current Pain Management Team, with customers and patients to provide clinical, technical support and education in the area of pain management/neuromodulation. * As a Clinical Specialist, your role will see you working in a medical environment and helping to manage cases. * This is a great role for a nurse or candidate with medical education to break into a commercial and clinical role, using your education and personality to build relationships with clinicians, patients etc * You will develop an excellent knowledge of three produc
Job Title: Sales and Clinical Support Specialist - Pain Management - Entry level - Reporting to the Sales Manager, you will be responsible for clinical support and selling as part of a team within the Pain Management portfolio. You will work closely with the current Pain Management Team, with customers and patients to provide clinical, technical support and education in the area of pain management/neuromodulation. * As a Clinical Specialist, your role will see you working in a medical environment and helping to manage cases. * This is a great role for a nurse or candidate with medical education to break into a commercial and clinical role, using your education and personality to build relationships with clinicians, patients etc * You will develop an excellent knowledge of three produc
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Or a clinical graduate looking to break into a sales support role? They are consistently ranked as a top employer, offering opportunities for clinical candidates to break into medical sales. Due to continued growth, they are now looking to hire a Clinical Support Specialist in Leinster to sell pain modulation portfolio to hospitals nationwide. THE ROLE: As the Clinical Sales Support, you will primarily focus on shadowing existing sales reps within this division, and conducting education sessions and demonstrations of the products within theatres. You will work alongside other clinical workers, support an account manager, and represent the company in hospital environments. * Clinical qualification is essential - Nurse, Physiotherapist, Podiatrist, Speech and Language S
Or a clinical graduate looking to break into a sales support role? They are consistently ranked as a top employer, offering opportunities for clinical candidates to break into medical sales. Due to continued growth, they are now looking to hire a Clinical Support Specialist in Leinster to sell pain modulation portfolio to hospitals nationwide. THE ROLE: As the Clinical Sales Support, you will primarily focus on shadowing existing sales reps within this division, and conducting education sessions and demonstrations of the products within theatres. You will work alongside other clinical workers, support an account manager, and represent the company in hospital environments. * Clinical qualification is essential - Nurse, Physiotherapist, Podiatrist, Speech and Language S
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We are currently recruiting for a Laboratory Technician for our Client, a construction material manufacturer based in Clonee, Co. Meath. This is a full-time temporary position, with the potential to become permanent. Full training will be provided. Maintaining rates of testing in accordance with relevant standards i.e. EN 196, EN15167; Ensuring product quality of incoming raw material. Sample, wash and grade aggregates; Test blocks and cubes of concrete; Recording and reporting of test results; Maintaining lab equipment, taking note of calibration; Maintaining inventory of lab equipment; Maintaining good housekeeping of lab. Strong attention to detail; Reliable and trustworthy; Good team player; Positive, friendly and flexible attitude to work. Monday to Friday 8am-4.30pm. €13.67 - €14.20 per hour depending on experience, with a 5% increase in July 2024. QED0369
We are currently recruiting for a Laboratory Technician for our Client, a construction material manufacturer based in Clonee, Co. Meath. This is a full-time temporary position, with the potential to become permanent. Full training will be provided. Maintaining rates of testing in accordance with relevant standards i.e. EN 196, EN15167; Ensuring product quality of incoming raw material. Sample, wash and grade aggregates; Test blocks and cubes of concrete; Recording and reporting of test results; Maintaining lab equipment, taking note of calibration; Maintaining inventory of lab equipment; Maintaining good housekeeping of lab. Strong attention to detail; Reliable and trustworthy; Good team player; Positive, friendly and flexible attitude to work. Monday to Friday 8am-4.30pm. €13.67 - €14.20 per hour depending on experience, with a 5% increase in July 2024. QED0369
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Clinical Chemistry / Haematology * Participate in the delivery of a quality laboratory service that supports the clinical needs of the hospital's patients - Histology Clinical Chemistry Haematology Microbiology
Clinical Chemistry / Haematology * Participate in the delivery of a quality laboratory service that supports the clinical needs of the hospital's patients - Histology Clinical Chemistry Haematology Microbiology
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Regulatory Affairs Officer - Permanent (Hybrid) About the client: Azon are delighted to be partnered with an Irish owned, family organisation which is well established in the market with over 30 years in business in the area. They are renowned for the supply of their niche products to EU customers. The successful candidate will have the opportunity to work on an 8 membered team, in a brand new role to the business in the management of dossiers for EU Regulatory Authority Approvals. North Dublin * Preparation and management of registration dossiers for approval by Regulatory Authorities. * Monitor the progress of Renewal and Re-Authorisation submissions. * Commission studies with Contract Research Organisations. Monitor progress of studies to ensure target dates are maintained. * Contribute towards development of Regulatory Strategy.
Regulatory Affairs Officer - Permanent (Hybrid) About the client: Azon are delighted to be partnered with an Irish owned, family organisation which is well established in the market with over 30 years in business in the area. They are renowned for the supply of their niche products to EU customers. The successful candidate will have the opportunity to work on an 8 membered team, in a brand new role to the business in the management of dossiers for EU Regulatory Authority Approvals. North Dublin * Preparation and management of registration dossiers for approval by Regulatory Authorities. * Monitor the progress of Renewal and Re-Authorisation submissions. * Commission studies with Contract Research Organisations. Monitor progress of studies to ensure target dates are maintained. * Contribute towards development of Regulatory Strategy.
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PE Global is currently recruiting for a Senior QC Analytical Analyst for a leading multi-national Pharma client based in Dublin. This is a 6 month maternity cover contract. * Responsibility for defining, scheduling, coordinating, and driving to completion of all QC required sections for Annual Product Quality Review (APQR) reports. * Responsibility for defining, scheduling, coordinating, and driving to completion all Annual Trend Reports. * Support harmonisation of trending across BMS network sites. Management of trend related investigations, in association with the QC Analytical Trending Lead. * Point of contact for internal and external manufacture sites, attend meetings where necessary. * Co-ordination of trend assessments with the relevant SMEs and ensure delivery to meet due dates. * Review trend limits from the manufacturing site and ensure timely implementation
PE Global is currently recruiting for a Senior QC Analytical Analyst for a leading multi-national Pharma client based in Dublin. This is a 6 month maternity cover contract. * Responsibility for defining, scheduling, coordinating, and driving to completion of all QC required sections for Annual Product Quality Review (APQR) reports. * Responsibility for defining, scheduling, coordinating, and driving to completion all Annual Trend Reports. * Support harmonisation of trending across BMS network sites. Management of trend related investigations, in association with the QC Analytical Trending Lead. * Point of contact for internal and external manufacture sites, attend meetings where necessary. * Co-ordination of trend assessments with the relevant SMEs and ensure delivery to meet due dates. * Review trend limits from the manufacturing site and ensure timely implementation
NPI validation troubleshooting production trials pharmaceuticals
NPI validation troubleshooting production trials pharmaceuticals
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Generation and management of change requests and associated actions on MasterControl. * Generation and management of non-conformances and associated actions on MasterControl. * Archiving and filing of CQV documentation associated with the project, including hard-copy and management of soft-copy archival on MasterControl.
Generation and management of change requests and associated actions on MasterControl. * Generation and management of non-conformances and associated actions on MasterControl. * Archiving and filing of CQV documentation associated with the project, including hard-copy and management of soft-copy archival on MasterControl.
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Supports the professional development and mentoring of Clinical Trial Manager Associates. Here, in Hays Life Sciences, our Multinational Clinical Trials client in Dublin is hiring a Clinical Trails Manager. They will work with the Clinical Program Manager and study teams to manage global clinical trials or regional components of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. * May serve as a resource for others within the company for clinical trials management expertise. * At least five years of relevant clinical
Supports the professional development and mentoring of Clinical Trial Manager Associates. Here, in Hays Life Sciences, our Multinational Clinical Trials client in Dublin is hiring a Clinical Trails Manager. They will work with the Clinical Program Manager and study teams to manage global clinical trials or regional components of global clinical trials and/or the entire process of a local clinical trial, with the ability to identify issues and adapt to changes. * May serve as a resource for others within the company for clinical trials management expertise. * At least five years of relevant clinical
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QC Analyst (Analytical Testing)
QC Analyst (Analytical Testing)
Recruitment by Aphex Group
Dunboyne, County Meath
€37,000 - €50,000 per annum
In our start-up site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and/or Analytical Methods. * Perform a variety of routine Analytical techniques and associated documentation; including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, Wet Chemistry methods in compliance with GMP requirements.
In our start-up site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and/or Analytical Methods. * Perform a variety of routine Analytical techniques and associated documentation; including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, Wet Chemistry methods in compliance with GMP requirements.
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Reporting to the QC Bioanalytical Manager, the successful candidate will be involved in assisting in laboratory operations, performing testing of samples and performing laboratory duties in accordance with cGMP regulations. * Assisting in updating and issuing documentation, including SOPs, as required * Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports * Accurately documenting laboratory work * Execute and assist in batch release testing, technical transfer and co-validation activities * Assisting with qualification of laboratory instruments * Perform instrument performance checks and calibration * Assist with troubleshooting of instrumentation * Data review based on demonstrated proficiency on assays * Experience in the following analytical techniques would be an advantage: Asepti
Reporting to the QC Bioanalytical Manager, the successful candidate will be involved in assisting in laboratory operations, performing testing of samples and performing laboratory duties in accordance with cGMP regulations. * Assisting in updating and issuing documentation, including SOPs, as required * Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports * Accurately documenting laboratory work * Execute and assist in batch release testing, technical transfer and co-validation activities * Assisting with qualification of laboratory instruments * Perform instrument performance checks and calibration * Assist with troubleshooting of instrumentation * Data review based on demonstrated proficiency on assays * Experience in the following analytical techniques would be an advantage: Asepti